Canonical Allele Identifier: CA377627197

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95556919T>A (hg19) ; chr10:g.93797162T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797162T>A , CM000672.2:g.93797162T>A	GRCh38
NC_000010.10:g.95556919T>A , CM000672.1:g.95556919T>A	GRCh37
NC_000010.9:g.95546909T>A	NCBI36
NG_011832.1:g.44354T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.1033T>A MANE Select	ENSP00000360472.4:p.Tyr345Asn
ENST00000485458.3:n.5009T>A
ENST00000635804.1:n.467T>A
ENST00000635953.1:c.*455T>A	ENSP00000490058.1:n.*455T>A
ENST00000636155.1:c.838+3812T>A	ENSP00000490355.1:n.838+3812T>A
ENST00000636232.1:c.*819T>A	ENSP00000490325.1:n.*819T>A
ENST00000636754.1:c.*875T>A	ENSP00000489781.1:n.*875T>A
ENST00000636946.1:c.*1008-587T>A	ENSP00000490654.1:n.*1008-587T>A
ENST00000637037.1:c.*623T>A	ENSP00000490860.1:n.*623T>A
ENST00000637347.1:n.894T>A
ENST00000637611.1:c.*589T>A	ENSP00000489682.1:n.*589T>A
ENST00000637689.1:c.-339T>A	ENSP00000490496.1:n.-339T>A
ENST00000637925.1:c.*628T>A	ENSP00000489763.1:n.*628T>A
ENST00000638049.1:c.*791T>A	ENSP00000490597.1:n.*791T>A
ENST00000676175.1:n.2772T>A
ENST00000371413.4:c.839-587T>A	ENSP00000360467.3:n.839-587T>A
ENST00000371418.8:c.1033T>A	ENSP00000360472.4:p.Tyr345Asn
ENST00000626307.1:n.4948T>A
ENST00000627420.2:c.*742T>A	ENSP00000487116.1:n.*742T>A
ENST00000629035.2:c.961T>A	ENSP00000486908.1:p.Tyr321Asn
ENST00000630047.2:c.889T>A	ENSP00000485917.1:p.Tyr297Asn
NM_001308275.1:c.839-587T>A	NP_001295204.1:n.839-587T>A
NM_001308276.1:c.889T>A	NP_001295205.1:p.Tyr297Asn
NM_005097.2:c.1033T>A	NP_005088.1:p.Tyr345Asn
NM_005097.3:c.1033T>A	NP_005088.1:p.Tyr345Asn
NR_131777.1:n.1297T>A
XM_017016912.2:c.695-587T>A	XP_016872401.1:n.695-587T>A
NM_005097.4:c.1033T>A MANE Select	NP_005088.1:p.Tyr345Asn
NM_001308275.2:c.839-587T>A	NP_001295204.1:n.839-587T>A
NM_001308276.2:c.889T>A	NP_001295205.1:p.Tyr297Asn
NR_131777.2:n.1170T>A